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鉴定对Ras(17N)生长抑制表型以及对Ras与鸟嘌呤核苷酸交换因子相互作用至关重要的残基。

Identification of residues critical for Ras(17N) growth-inhibitory phenotype and for Ras interaction with guanine nucleotide exchange factors.

作者信息

Quilliam L A, Kato K, Rabun K M, Hisaka M M, Huff S Y, Campbell-Burk S, Der C J

机构信息

Department of Pharmacology, University of North Carolina at Chapel Hill School of Medicine 27599.

出版信息

Mol Cell Biol. 1994 Feb;14(2):1113-21. doi: 10.1128/mcb.14.2.1113-1121.1994.

Abstract

The Ras(17N) dominant negative antagonizes endogenous Ras function by forming stable, inactive complexes with Ras guanine nucleotide exchange factors (GEFs; e.g., SOS1). We have used the growth-inhibitory phenotype of Ras(17N) to characterize two aspects of Ras interaction with GEFs. First, we used a nonprenylated version of Ras(17N), designated Ras(17N/186S), which no longer associates with the plasma membrane and lacks the growth-inhibitory phenotype, to address the importance of Ras subcellular location and posttranslational modification for its interaction with GEFs. We observed that addition of an N-terminal myristylation signal to Ras(17N/186S) restored the growth-inhibitory activity of nonprenylated Ras(17N). Thus, membrane association, rather than prenylation, is critical for Ras interaction with Ras GEFs. Second, we used a biological selection approach to identify Ras residues which are critical for Ras(17N) growth inhibition and hence for interaction with Ras GEFs. We identified mutations at residues 75, 76, and 78 that abolished the growth-inhibitory activity of Ras(17N). Since GEF interaction is dispensable for oncogenic but not normal Ras function, our demonstration that single-amino-acid substitutions at these three positions impaired the transforming activity of normal but not oncogenic Ras provides further support for the role of these residues in Ras-GEF interactions. Finally, Ras(WT) proteins with mutations at these residues were no longer activated by mammalian SOS1. Altogether, these results suggest that the Ras intracellular location and Ras residues 75 to 78 are critical for Ras-GEF interaction.

摘要

Ras(17N)显性负性突变体通过与Ras鸟嘌呤核苷酸交换因子(GEFs;如SOS1)形成稳定的无活性复合物来拮抗内源性Ras功能。我们利用Ras(17N)的生长抑制表型来表征Ras与GEFs相互作用的两个方面。首先,我们使用了一种非异戊二烯化形式的Ras(17N),命名为Ras(17N/186S),它不再与质膜结合且缺乏生长抑制表型,以探讨Ras亚细胞定位和翻译后修饰对其与GEFs相互作用的重要性。我们观察到,向Ras(17N/186S)添加N端肉豆蔻酰化信号可恢复非异戊二烯化Ras(17N)的生长抑制活性。因此,膜结合而非异戊二烯化对于Ras与Ras GEFs的相互作用至关重要。其次,我们采用生物学筛选方法来鉴定对Ras(17N)生长抑制至关重要且因此对与Ras GEFs相互作用至关重要的Ras残基。我们鉴定出75、76和78位残基的突变消除了Ras(17N)的生长抑制活性。由于GEF相互作用对于致癌性Ras功能而非正常Ras功能是可有可无的,我们证明这三个位置的单氨基酸取代损害了正常而非致癌性Ras的转化活性,这进一步支持了这些残基在Ras-GEF相互作用中的作用。最后,这些残基发生突变的Ras(WT)蛋白不再被哺乳动物SOS1激活。总之,这些结果表明Ras的细胞内定位以及Ras的75至78位残基对于Ras-GEF相互作用至关重要。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/549d/358467/3da15a4b65f0/molcellb00002-0257-a.jpg

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